40318-29-4

Basic information

• Product Name: (3,4-dimethyl-phenyl)-carbamic acid ethyl ester
• Synonyms: (3,4-dimethyl-phenyl)-carbamic acid ethyl ester
• CAS NO: 40318-29-4
• Molecular Weight: 193.246
• Mol File: 40318-29-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (3,4-dimethyl-phenyl)-carbamic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (3,4-dimethyl-phenyl)-carbamic acid ethyl ester(40318-29-4)
• EPA Substance Registry System: (3,4-dimethyl-phenyl)-carbamic acid ethyl ester(40318-29-4)

Safety Data

• Hazardous Substances Data: 40318-29-4(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 541-41-3 chloroformic acid ethyl ester 
• 95-64-7 4-amino-o-xylene 
• 619-04-5 3,4-dimethylbenzoic acid 

Downstream Products

• 40318-30-7 (3,4-dimethyl-2,6-dinitro-phenyl)-carbamic acid ethyl ester 
• 847819-97-0 (3,4-dimethyl-2-nitro-phenyl)-carbamic acid ethyl ester 
• 40318-31-8 3,4-dimethyl-2,6-dinitroaniline 
• 64823-23-0 3,4-Dimethyl-2-nitroanilin 
• 380635-86-9 acetic acid-(3,4-dimethyl-2-nitro-anilide) 
• 40318-47-6 N-Isopropyl-3,4-dimethyl-2,6-dinitroaniline 
• 40318-32-9 1-Chloro-3,4-dimethyl-2,6-dinitrobenzene 
• 40318-45-4 N-(2-butyl)-3,4-dimethyl-2,6-dinitroaniline 

Relevant articles and documents

Synthesis of 3,4-benzo-7-hydroxy-2,9-diazabicyclo[3.3.1]non-7-enes by cyclization of 1,3-bis(silyl enol ethers) with quinazolines

A variety of functionalized 3,4-benzo-7-hydroxy-2,9-diazabicyclo[3.3.1]non- 7-enes were prepared by one-pot cyclizations of 1,3-bis(silyl enol ethers) with quinazolines. The mechanism of the cyclization was studied by B3LYP/6-31G(d) density functional theory computations. The products could be functionalized by Suzuki cross-coupling reactions. The reaction of 1,3-bis(silyl enol ethers) with phthalazine afforded open-chain rather than cyclization products. The Royal Society of Chemistry.